99mTc pyrene derivative complex causes double-strand breaks in dsDNA mainly through cluster-mediated indirect effect in aqueous solution

Wei Ju Chung, Yujia Cui, Feng Yun J Huang, Tzu Hui Tu, Tzu Sen Yang, Jem Mau Lo, Chi Shiun Chiang, Ian C. Hsu

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Radiation therapy for cancer patients works by ionizing damage to nuclear DNA, primarily by creating double-strand breaks (DSB). A major shortcoming of traditional radiation therapy is the set of side effect associated with its long-range interaction with nearby tissues. Low-energy Auger electrons have the advantage of an extremely short effective range, minimizing damage to healthy tissue. Consequently, the isotope 99mTc, an Auger electron source, is currently being studied for its beneficial potential in cancer treatment. We examined the dose effect of a pyrene derivative 99mTc complex on plasmid DNA by using gel electrophoresis in both aqueous and methanol solutions. In aqueous solutions, the average yield per decay for double-strand breaks is 0.011±0.005 at low dose range, decreasing to 0.0005±0.0003 in the presence of 1 M dimethyl sulfoxide (DMSO). The apparent yield per decay for single-strand breaks (SSB) is 0.04±0.02, decreasing to approximately a fifth with 1 M DMSO. In methanol, the average yield per decay of DSB is 0.54±0.06 and drops to undetectable levels in 2 M DMSO. The SSB yield per decay is 7.2±0.2, changing to 0.4±0.2 in the presence of 2 M DMSO. The 95% decrease in the yield of DSB in DMSO indicates that the main mechanism for DSB formation is through indirect effect, possibly by cooperative binding or clustering of intercalators. In the presence of non-radioactive ligands at a near saturation concentration, where radioactive Tc compounds do not form large clusters, the yield of SSB stays the same while the yield of DSB decreases to the value in DMSO. DSBs generated by 99mTc conjugated to intercalators are primarily caused by indirect effects through clustering.

Original languageEnglish
Article numbere108162
JournalPLoS One
Volume9
Issue number9
DOIs
Publication statusPublished - Sep 22 2014

Fingerprint

Dimethyl Sulfoxide
aqueous solutions
dimethyl sulfoxide
chemical derivatives
Derivatives
Intercalating Agents
deterioration
Radiotherapy
radiotherapy
Cluster Analysis
Methanol
Electrons
Tissue
methanol
Electron sources
electrons
Oncology
DNA
neoplasms
Electrophoresis

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

99mTc pyrene derivative complex causes double-strand breaks in dsDNA mainly through cluster-mediated indirect effect in aqueous solution. / Chung, Wei Ju; Cui, Yujia; Huang, Feng Yun J; Tu, Tzu Hui; Yang, Tzu Sen; Lo, Jem Mau; Chiang, Chi Shiun; Hsu, Ian C.

In: PLoS One, Vol. 9, No. 9, e108162, 22.09.2014.

Research output: Contribution to journalArticle

Chung, Wei Ju ; Cui, Yujia ; Huang, Feng Yun J ; Tu, Tzu Hui ; Yang, Tzu Sen ; Lo, Jem Mau ; Chiang, Chi Shiun ; Hsu, Ian C. / 99mTc pyrene derivative complex causes double-strand breaks in dsDNA mainly through cluster-mediated indirect effect in aqueous solution. In: PLoS One. 2014 ; Vol. 9, No. 9.
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